Myopia control with orthokeratology lenses. A 3-year follow-up study including a cross-over design: Clinical study Of Near-sightedness; TReatment with Orthokeratology Lenses 2 (CONTROL2 study).

IF 3 3区 医学 Q1 OPHTHALMOLOGY
T M Jakobsen, K B Høeg, F Møller
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Abstract

Purpose: The purpose of this study is to investigate 3-year efficacy of orthokeratology lenses (OKL) in controlling axial length progression in myopic Scandinavian children. Through a cross-over design of the control group to compare the treatment efficacy in younger versus older children, with the latter having higher cycloplegic spherical refractive error (cSEQ) at treatment initiation. Further, the study aimed to evaluate the safety of the treatment.

Methods: This was a continuation of the randomized controlled study Clinical study Of Near-sightedness; TReatment with Orthokeratology Lenses (CONTROL study) in which the follow-up period of the original intervention group, that received OKL, was extended from 18 months to 36 months. Meanwhile, the original control group was crossed-over to OKL after the 18-month follow-up visit and treated for 18 months. Biometry was measured using Lenstar LS900, and contact lens complications were graded according to Efron Grading Scale for Contact Lens Complications (Efron score). Mixed models were used for statistical analysis.

Results: Nineteen subjects in the OKL group and 28 in the control group completed the CONTROL study. Hereof, 17 and 24 subjects from the OKL group and control group, respectively, agreed to participate in the CONTROL2 study. In the OKL continue group, the treatment efficacy did not decline during the 3-year study period (p-values for follow-up visits were all ≥0.82). There was no statistically significant difference between treatment efficacy when OKL treatment was initiated in younger versus older children (p-value ≥0.14 for all follow-up visits). Low-grade corneal staining was seen in several subjects at some point during the study, but here were no treatment-requiring or sight-threatening adverse events during the study period.

Conclusion: The efficacy of myopia control by OKL was stable during 3 years of treatment. Similar treatment efficacies were found regardless of the age at treatment initiation. No severe adverse events occurred during the study period.

使用角膜塑形镜控制近视。一项为期 3 年的随访研究,包括一项交叉设计:近视临床研究;角膜塑形镜治疗 2(CONTROL2 研究)。
目的:本研究旨在调查角膜塑形镜(OKL)在控制斯堪的纳维亚近视儿童轴长增长方面的 3 年疗效。通过对照组的交叉设计,比较年龄较小的儿童与年龄较大的儿童的疗效,其中年龄较大的儿童在开始治疗时的球面屈光不正(cSEQ)较高。此外,该研究还旨在评估治疗的安全性:本研究是随机对照研究 "近视临床研究;角膜塑形镜治疗"(CONTROL 研究)的延续,其中接受角膜塑形镜治疗的原干预组的随访期从 18 个月延长至 36 个月。与此同时,原来的对照组在 18 个月的随访后交叉使用 OKL,并治疗 18 个月。使用 Lenstar LS900 测量生物测量值,并根据隐形眼镜并发症埃夫隆分级表(埃夫隆评分)对隐形眼镜并发症进行分级。统计分析采用混合模型:结果:19 名 OKL 组受试者和 28 名对照组受试者完成了 CONTROL 研究。其中,OKL组和对照组分别有17名和24名受试者同意参加CONTROL2研究。在 OKL 继续治疗组中,治疗效果在 3 年的研究期间没有下降(随访的 p 值均≥0.82)。年龄较小的儿童和年龄较大的儿童在开始 OKL 治疗时的疗效没有明显的统计学差异(所有随访的 p 值均≥0.14)。在研究过程中,几名受试者的角膜曾出现低度染色,但在研究期间没有出现需要治疗或危及视力的不良反应:结论:OKL 控制近视的疗效在 3 年的治疗过程中保持稳定。结论:OKL 控制近视的疗效在 3 年的治疗中保持稳定,无论开始治疗时的年龄如何,疗效都相似。研究期间未发生严重不良事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Ophthalmologica
Acta Ophthalmologica 医学-眼科学
CiteScore
7.60
自引率
5.90%
发文量
433
审稿时长
6 months
期刊介绍: Acta Ophthalmologica is published on behalf of the Acta Ophthalmologica Scandinavica Foundation and is the official scientific publication of the following societies: The Danish Ophthalmological Society, The Finnish Ophthalmological Society, The Icelandic Ophthalmological Society, The Norwegian Ophthalmological Society and The Swedish Ophthalmological Society, and also the European Association for Vision and Eye Research (EVER). Acta Ophthalmologica publishes clinical and experimental original articles, reviews, editorials, educational photo essays (Diagnosis and Therapy in Ophthalmology), case reports and case series, letters to the editor and doctoral theses.
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